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SRX7391409: Flow-Seq of GFP library with intron in HeLa cells
1 ILLUMINA (Illumina MiSeq) run: 1.3M spots, 748.3M bases, 359.9Mb downloads

Design: To prepare Flow-Seq libraries, cells were FACS sorted by GFP fluorescence into eight bins, followed by genomic DNA isolation and PCR with primers specific to GFP 5'- and 3'-UTR sequences
Submitted by: University of Edinburgh
Study: Splicing buffers suboptimal codon usage in human cells
show Abstracthide Abstract
We measured the effects of splicing on expression in a panel of synonymous variants of GFP and mKate2 reporter genes that varied in nucleotide composition. We found that splicing promotes the expression of adenine and thymine (AT)-rich variants by increasing their steady-state protein and mRNA levels, in part through promoting cytoplasmic localization of mRNA. Splicing had little or no effect on the expression of guanine and cytosine (GC)-rich variants.
Sample:
SAMN13612109 • SRS5839594 • All experiments • All runs
Organism: synthetic gene
Library:
Name: CM9b_Bin2
Instrument: Illumina MiSeq
Strategy: AMPLICON
Source: SYNTHETIC
Selection: PCR
Layout: PAIRED
Runs: 1 run, 1.3M spots, 748.3M bases, 359.9Mb
Run# of Spots# of BasesSizePublished
SRR107145331,251,318748.3M359.9Mb2021-01-01

ID:
9677131

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